Human Phenotype Ontology 
Grandparent Node:
Abnormality of the tongue (HP:0000157)help
Parent Node:
Abnormal tongue morphology (HP:0030809)help
..Starting node
Geographic tongue (HP:0025252)help
Term ID: 25252
Name: Geographic tongue
Synonym: Annulus migrans; Benign migratory glossitis; Glossitis areata exfoliativa; Lingual erythema migrans; Wandering rash of the tongue
Definition: An anomaly of the tongue characterized by loss (atrophy) of filiform papillae of the tongue, leaving areas of erythema (redness), surrounded by a serpiginous, white, hyperkeratotic border. The name geographic tongue refers to an appearance that is said to be similar to a map.
Reference: HP:0025252
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal hyoglossus muscle morphology (HP:3000051) help
..expandAbnormal lingual artery morphology (HP:3000074) help
..expandAbnormality of lingual tonsil (HP:3000076) help
..expandAbnormality of the tongue muscle (HP:0040173) help
..expandAnkyloglossia (HP:0010296) help
..expandAplasia/Hypoplasia of the tongue (HP:0010295) help
..expandBifid tongue (HP:0010297) help
..expandDuplicated tongue (HP:0040294) help
..expandFurrowed tongue (HP:0000221) help
..expandGlossitis (HP:0000206) help
..expandGlossoptosis (HP:0000162) help
..expandLobulated tongue (HP:0000180) help
..expandMacroglossia (HP:0000158) help
..expandPosteriorly placed tongue (HP:0009087) help
..expandProtruding tongue (HP:0010808) help
..expandSmooth tongue (HP:0010298) help
..expandStiff tongue (HP:0031373) help
..expandStrawberry tongue (HP:0031042) help
..expandTongue atrophy (HP:0012473) help
..expandTongue nodules (HP:0000199) help
..expandTongue telangiectasia (HP:0000227) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025252HP:0025252Geographic tongue0IL36RN CL E G H2652515561OMIM:614204PSORIASIS 14, PUSTULAR; PSORS1451

Genes (1) :IL36RN

Diseases (1) :OMIM:614204

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.